Canonical Allele Identifier: CA973101949
Gene:

Linked Data

dbSNP Id: rs1899532921

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.95782475T>A , CM000677.2:g.95782475T>A GRCh38
NC_000015.9:g.96325704T>A , CM000677.1:g.96325704T>A GRCh37
NC_000015.8:g.94126708T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_932654.1:n.148-42714T>A